Detection of gene-environment interactions in a family-based population using SCAD

2017 ◽  
Vol 36 (22) ◽  
pp. 3547-3559 ◽  
Author(s):  
Gwangsu Kim ◽  
Chao-Qiang Lai ◽  
Donna K. Arnett ◽  
Laurence D. Parnell ◽  
Jose M. Ordovas ◽  
...  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Chao-Yu Guo ◽  
Reng-Hong Wang ◽  
Hsin-Chou Yang

AbstractAfter the genome-wide association studies (GWAS) era, whole-genome sequencing is highly engaged in identifying the association of complex traits with rare variations. A score-based variance-component test has been proposed to identify common and rare genetic variants associated with complex traits while quickly adjusting for covariates. Such kernel score statistic allows for familial dependencies and adjusts for random confounding effects. However, the etiology of complex traits may involve the effects of genetic and environmental factors and the complex interactions between genes and the environment. Therefore, in this research, a novel method is proposed to detect gene and gene-environment interactions in a complex family-based association study with various correlated structures. We also developed an R function for the Fast Gene-Environment Sequence Kernel Association Test (FGE-SKAT), which is freely available as supplementary material for easy GWAS implementation to unveil such family-based joint effects. Simulation studies confirmed the validity of the new strategy and the superior statistical power. The FGE-SKAT was applied to the whole genome sequence data provided by Genetic Analysis Workshop 18 (GAW18) and discovered concordant and discordant regions compared to the methods without considering gene by environment interactions.


2018 ◽  
Vol 8 (1) ◽  
pp. 10 ◽  
Author(s):  
S. Shiao ◽  
James Grayson ◽  
Chong Yu ◽  
Brandi Wasek ◽  
Teodoro Bottiglieri

Oncotarget ◽  
2018 ◽  
Vol 9 (49) ◽  
pp. 29019-29035 ◽  
Author(s):  
Mildred C. Gonzales ◽  
James Grayson ◽  
Amanda Lie ◽  
Chong Ho Yu ◽  
Shyang-Yun Pamela K. Shiao

2006 ◽  
Vol 114 (10) ◽  
pp. 1547-1552 ◽  
Author(s):  
Abee L. Boyles ◽  
Ashley V. Billups ◽  
Kristen L. Deak ◽  
Deborah G. Siegel ◽  
Lorraine Mehltretter ◽  
...  

2017 ◽  
Vol 37 (3) ◽  
pp. 506-506
Author(s):  
Gwangsu Kim ◽  
Chao-Qiang Lai ◽  
Donna K. Arnett ◽  
Laurence D. Parnell ◽  
Jose M. Ordovas ◽  
...  

Biometrics ◽  
2008 ◽  
Vol 64 (2) ◽  
pp. 458-467 ◽  
Author(s):  
Stijn Vansteelandt ◽  
Dawn L. DeMeo ◽  
Jessica Lasky-Su ◽  
Jordan W. Smoller ◽  
Amy J. Murphy ◽  
...  

2013 ◽  
Vol 33 (2) ◽  
pp. 304-318 ◽  
Author(s):  
Weiming Zhang ◽  
Carl D. Langefeld ◽  
Gary K. Grunwald ◽  
Tasha E. Fingerlin

2016 ◽  
Vol 10 (S7) ◽  
Author(s):  
Lindsay Fernández-Rhodes ◽  
Chani J. Hodonsky ◽  
Mariaelisa Graff ◽  
Shelly-Ann M. Love ◽  
Annie Green Howard ◽  
...  

2016 ◽  
Author(s):  
BENJAMIN W DOMINGUE ◽  
Jason D. Boardman

We use genome-wide data from the third generation respondents of the Framingham Heart Study to estimate heritability in body mass index using different quantities of the measured genotype. Heritability decreases rapidly when SNPs implicated by a genome-wide association study are removed but shows essentially no decline when SNPs implicated by a gene-environment interaction in a second genome-wide analysis are removed. This second result is highlighted by our additional finding that the SNPs which explain heritability amongst a subsample defined by higher educational attainment explain no heritability of the heritability in the lower education group, and vice-versa. Finally, we do find consistent heritability estimates when we compare family-based estimates versus those based on measured genotype.


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